@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_head
{
this:
np:hasAssertion
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_assertion
;
np:hasProvenance
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_assertion
a
np:Assertion
.
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_provenance
a
np:Provenance
.
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_assertion
{
miriam-gene:94
a
ncit:C16612
.
lld:C0152171
a
ncit:C7057
.
dgn-gda:DGNc74df5bba6d7f983245689f5f2100e78
sio:SIO_000628
miriam-gene:94
,
lld:C0152171
;
a
sio:SIO_001121
.
}
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_provenance
{
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_assertion
dcterms:description
"[Heritable and idiopathic pulmonary arterial hypertension (PAH) are phenotypically identical and associated with mutations in several genes related to transforming growth factor (TGF) beta signaling, including bone morphogenetic protein receptor type 2, activin receptor-like kinase 1, endoglin, and mothers against decapentaplegic 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22474227
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP427582.RAB2BJx6OZkzelQ1-vDw4jhostpM2mg-JWBf1MeUpCYDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}